ENST00000328300.11:c.4860A>G
MANE Select
|
ENSP00000331902.7:p.Leu1620=
|
|
ENST00000361603.7:c.4842A>G
|
ENSP00000354505.2:p.Leu1614=
|
|
ENST00000510690.2:n.1354A>G
|
|
|
ENST00000644079.1:n.1691A>G
|
|
|
ENST00000328300.10:c.4860A>G
|
ENSP00000331902.6:p.Leu1620=
|
|
ENST00000361603.6:c.4842A>G
|
ENSP00000354505.2:p.Leu1614=
|
|
ENST00000504541.1:c.219+384A>G
|
ENSP00000424845.1:n.219+384A>G
|
|
ENST00000515658.1:c.325-992A>G
|
|
|
NM_000495.4:c.4842A>G
|
NP_000486.1:p.Leu1614=
|
|
NM_033380.2:c.4860A>G
|
NP_203699.1:p.Leu1620=
|
|
XM_005262070.2:c.4851A>G
|
XP_005262127.1:p.Leu1617=
|
|
XM_006724616.2:c.4860A>G
|
XP_006724679.1:p.Leu1620=
|
|
XM_011530849.1:c.4536A>G
|
XP_011529151.1:p.Leu1512=
|
|
XM_011530851.1:c.2433A>G
|
XP_011529153.1:p.Leu811=
|
|
XM_011530849.2:c.4875A>G
|
XP_011529151.2:p.Leu1625=
|
|
XM_017029259.2:c.4866A>G
|
XP_016884748.1:p.Leu1622=
|
|
XM_017029260.1:c.4857A>G
|
XP_016884749.1:p.Leu1619=
|
|
XM_017029263.2:c.3195A>G
|
XP_016884752.1:p.Leu1065=
|
|
NM_000495.5:c.4842A>G
|
NP_000486.1:p.Leu1614=
|
|
NM_033380.3:c.4860A>G
MANE Select
|
NP_203699.1:p.Leu1620=
|
|